Stakeholder Involvement in the Development of a New Proactive Clinical Review of Patients Prescribed Opioid Medicines Long-Term for Persistent Pain in Primary Care

IF 3 3区 医学 Q2 HEALTH CARE SCIENCES & SERVICES
Sarah A. Harrisson, Clare Jinks, Nicola Cornwall, Charlotte Woodcock, Lisa Dikomitis, Toby Helliwell, Adele Higginbottom, Janet Lefroy, Roger Knaggs, Tamar Pincus, Miriam Santar, Claire Sillitto, Matthew Webb, Simon White, Christian D. Mallen, Julie Ashworth
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引用次数: 0

Abstract

Background

Stakeholder involvement is a core element of the Medical Research Council (MRC) framework for developing and evaluating complex interventions, but approaches to involve stakeholders are not well-reported. We outline how stakeholders contributed to co-designing a Proactive clinical Review of patients taking Opioid Medicines long-term for persistent Pain led by Pharmacists working in primary care Teams (the PROMPPT intervention—a review and pharmacist training package).

Methods

We brought key stakeholders together to co-design the PROMPPT intervention using a person-based approach, alongside evidence from best practice guidance. We established a community of practice comprising three complementary groups: a patient advisory group, a pharmacist advisory group and a mixed stakeholder group. Patient stakeholders were identified from an existing patient involvement group. Professional stakeholders were identified using networks and social media. The three groups met in iterative workshops with predefined aims. We offered reimbursement for the stakeholders' time.

Outcomes

The patient advisory group (n = 10), pharmacist advisory group (n = 6) and mixed stakeholder group (n = 16) each met for 2 or 3 workshops between April 2019 and February 2020. Stakeholders had expertise, often cross-cutting, in lived experience, persistent pain, opioids, delivering primary healthcare and/or promoting behaviour change. Patient stakeholders provided their perspectives of consulting about their pain and opioids. Pharmacist stakeholders provided their perspectives on how pain reviews were happening in practice and on considerations for training (e.g., vignettes and experiential learning were considered important). The mixed stakeholder group provided a breadth of views highlighting current practice, including the value of engaging the wider GP practice team, issues around clinical responsibility for prescribing and the fact that international clinical guidance was not always relevant to UK primary care.

Conclusions

By understanding the context of the PROMPPT intervention, stakeholders worked to develop a new pharmacist-led primary care review ahead of feasibility testing. We make recommendations for future developers of complex interventions.

Patient and Public Contribution

Patient stakeholders, including a lay co-applicant (C.S.) supported by a PPI support worker (A.H.), helped develop and refine the intervention. C.S. and A.H. read and contributed to the initial manuscript and approved the final manuscript.

Abstract Image

利益相关者参与开发一项新的前瞻性临床综述,该综述针对初级保健中长期开具阿片类药物治疗持续性疼痛的患者
利益攸关方的参与是医学研究理事会制定和评估复杂干预措施框架的核心要素,但涉及利益攸关方的方法没有得到很好的报道。我们概述了利益相关者如何共同设计由初级保健团队工作的药剂师领导的长期服用阿片类药物治疗持续性疼痛的患者的前瞻性临床审查(PROMPPT干预-审查和药剂师培训包)。方法:我们将主要利益相关者召集在一起,采用以人为本的方法,并结合最佳实践指南的证据,共同设计PROMPPT干预措施。我们建立了一个由三个互补小组组成的实践社区:患者咨询小组,药剂师咨询小组和混合利益相关者小组。从现有的患者参与组中确定患者利益相关者。通过网络和社交媒体确定专业利益相关者。这三个小组以预先确定的目标在迭代的研讨会中会面。我们为涉众的时间提供补偿。在2019年4月至2020年2月期间,患者咨询小组(n = 10)、药剂师咨询小组(n = 6)和混合利益相关者小组(n = 16)分别召开了2至3次研讨会。利益攸关方在生活经验、持续性疼痛、类阿片、提供初级保健和/或促进行为改变等方面具有专业知识,往往是跨领域的。患者利益相关者提供了他们对疼痛和阿片类药物咨询的看法。药剂师利益相关者提供了他们对疼痛评估在实践中是如何发生的观点,以及对培训的考虑(例如,小插曲和经验学习被认为是重要的)。混合利益相关者小组提供了广泛的观点,突出了当前的实践,包括参与更广泛的全科医生实践团队的价值,关于处方临床责任的问题,以及国际临床指导并不总是与英国初级保健相关的事实。通过了解PROMPPT干预的背景,利益相关者致力于在可行性测试之前开发一种新的由药剂师主导的初级保健审查。我们为未来复杂干预措施的开发者提出建议。患者利益相关者,包括由PPI支持工作者(A.H.)支持的外行共同申请人(C.S.),帮助开发和完善了干预措施。C.S.和A.H.阅读并参与了初稿,并批准了最终稿。
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来源期刊
Health Expectations
Health Expectations 医学-公共卫生、环境卫生与职业卫生
CiteScore
5.20
自引率
9.40%
发文量
251
审稿时长
>12 weeks
期刊介绍: Health Expectations promotes critical thinking and informed debate about all aspects of patient and public involvement and engagement (PPIE) in health and social care, health policy and health services research including: • Person-centred care and quality improvement • Patients'' participation in decisions about disease prevention and management • Public perceptions of health services • Citizen involvement in health care policy making and priority-setting • Methods for monitoring and evaluating participation • Empowerment and consumerism • Patients'' role in safety and quality • Patient and public role in health services research • Co-production (researchers working with patients and the public) of research, health care and policy Health Expectations is a quarterly, peer-reviewed journal publishing original research, review articles and critical commentaries. It includes papers which clarify concepts, develop theories, and critically analyse and evaluate specific policies and practices. The Journal provides an inter-disciplinary and international forum in which researchers (including PPIE researchers) from a range of backgrounds and expertise can present their work to other researchers, policy-makers, health care professionals, managers, patients and consumer advocates.
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